Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
  • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
  • C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
  • A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
  • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
  • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
  • C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
  • C07D213/54—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
  • C07D213/55—Acids; Esters
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
  • C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
  • C07D409/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms

Definitions

• the present invention is directed to a new class of 3,3-bisthioalkyl-2-pyridylacrylic acid derivatives, particularly the esters, which are useful as fungicides.
• phytopathogenic fungi The control of phytopathogenic fungi is of great economic importance since fungal growth on plants or on parts of plants such as fruits, blossoms, foliage, stems, tubers, roots and the like not only inhibits production of a plant as well as commercially
• fungicidal compositions containing malonic esters including the commercial fungicide Isoprothiolane (di-isopropyl 1,3-dithiolane-2ylidenemalonate): C
• Compound (A) is for practical purposes a "one-species" fungicide, being effective at economic rates only against
• One aspect of the present invention is a new class of compounds having the structural formula
• R and R 1 are each independently members selected from the group consisting of
• R 2 is C 1 -C 5 alkyl.
• the present invention is also directed .to fungicidal compositions comprising (A) a fungicidally effective amount of at least one compound having structure (I) above, and (B) an agriculturally acceptable carrier. Further, the present invention is directed to a process for controlling
• the compounds of the present invention may be prepared by reacting an alkyl 3-pyridylacetate having the structural formula (II)
• R 2 is as defined above, with carbon disulfide in the presence of a base such as potassium hydroxide in a polar solvent, preferably dimethyl sulfoxide.
• a base such as potassium hydroxide in a polar solvent, preferably dimethyl sulfoxide. The reaction occurs at room temperature over a period of from 6-18 hours.
• the preferred stoichiometric ratio of the reactants which results in the formation of the desired compound having the structural formula I is one molar equivalent of the alkyl 3-pyridylacetate having the structural formula II to a slight excess of one molar equivalent of carbon disulfide and two molar equivalents of the alkyl halide having the structural formula III.
• the desired compound (formula I) is isolated by pouring into water, extracting with several portions of chloroform, subsequent evaporation of the chloroform, chromatography on alumina, eluting with chloroform and finally evaporation of the chloroform.
• the compounds in this invention have structures represented by formula (I) and stereoisomers thereof, where R and R 1 are each independently a substituent or group of substituents representing C 1 -C 10 alkyl; benzyl;
• R 2 is methyl, ethyl, isopropyl or n-pentyl. Preferred is R
• R + R 1 equals a total of 6 to 9 non-hydrogen atoms and at least one of R + R 1 containing a C-C double bond. Less preferred are compounds in which the two sulfur atoms are placed in a ring, i.e., R + R 1 equals alkylene, as those compounds are generally less active than compounds in which the two sulfur atoms are not in a ring.
• Particularly preferred compounds include:
• Preferred compositions include at least one preferred compound described above.
• composition of the present invention includes, as one component thereof, a carrier suitable for
• the carrier may be solid, for example, finely divided particulate solids, granules, pellets, wettable powders, soluble powders and the like.
• the solid carriers within the contemplation of the subject invention are organic and inorganic materials such as attapulgite clay, sand, vermiculite, corncob, activated carbon and mineral silicates.
• the mineral silicates preferred for use in the composition of the present invention are mica, talc, pyrophyllite, clays and the like.
• a solid composition may be prepared from a solid carrier, such as one of those described immediately above.
• the active compound is impregnated onto the solid carrier.
• the active compound may be formulated into a wettable powder by grinding it into a fine powder and mixing it with the solid carrier to which a surface active dispersing agent has been added. The wettable powder is then dispersed in water and applied as a dispersion.
• the liquid composition may be in the form of a solution or an emulsion.
• the active ingredient is dissolved in an aqueous or organic solvent.
• the solvent which acts as the carrier, is organic.
• other preferred solvents include such organic compounds as acetone, methanol, isopropanol, t-butyl alcohol, cyclohexanone, dioxane, dimethylformamide, dimethyl sulfoxide, ethylene dichloride, diacetone alcohol and
• a water emulsion another preferred embodiment of a liquid composition within the contemplation of the present invention, is prepared from a solution, as described above, to which a surface active agent is added.
• a surface active agent suitable for use in forming an emulsion within the contemplation of this invention are known to those skilled in the art.
• the surface active agent may be anionic, non-ionic or cationic.
• the carrier component of the present composition may also be an aerosol.
• an aerosol the active compound is dissolved in a non-highly volatile solvent. This solution is then admixed with a highly volatile solvent, a so-called liquid aerosol carrier.
• the aerosol carrier is liquid only under elevated pressure. At ambient temperature and pressure, the aerosol carrier is a gas. In a subembodiment of this preferred carrier, the aerosol carrier may itself be active.
• the carrier may be an insecticide, a herbicide, a bacteriacide or the like.
• the compounds and compositions of the present invention may be used in methods for controlling phytopathogenic fungi. In those methods, a fungicidally effective amount of the active ingredient, whether in compound or composition form, is applied to the locus under attack by fungi.
• the active ingredient is applied to the locus under attack by the fungi by application to the foliage of the plants to be
• a fungicidally effective amount of the active ingredient is applied to the soil in which the plants to be protected are grown.
• the active ingredient is applied to the soil in which the plant to be protected is grown in a concentration of between abut 0.125 and about 10 kilograms per hectare
• systemic control involves application of between about 1.125 kg/ha to about 5 kg/ha.
• controlling fungi is utilized, either the foliar or systemic treatment, the active ingredient may be applied prior to or after infection by fungi. Furthermore, it should be appreciated that the exact dosage, applied systemically or to the foliage, is dictated by the fungus to be controlled and the particular plant to be protected.
• the active ingredient is applied as a coating to the seeds of the plant to be protected.
• fungicidal coating protects the soil from the infection by the fungi and is also taken up the plant systemically to protect the plant from fungal attack.
• seed coating method an appropriate
• concentration of the active ingredient is in the range of between about 5 and 75 grams per hundred kilograms of seed.
• Allyl bromide (8.47 grams, 70.0 mmoles) was added during ninety minutes in four approximately equal portions. The reaction mixture was stirred at room temperature overnight and then poured into 1600 ml of water. The mixture was extracted with three 35-ml portions of chloroform. The chloroform extracts were combined and washed with two 1500-ml portions of water.
• the mixture was stirred without heating for 3.5 hours.
• the maximum temperature, attained after one hour, was 34.5°C.
• compositions were formed into compositions. This was accomplished by dissolving 0.3 grams of each of the compounds in 10 ml of acetone or other suitable solvent. Each of these solutions were treated with 1 to 2 drops of an emulsifying agent, such as Triton [trademark] X-100, and water was added to form an emulsion. The degree of dilution with water was dictated by the desired concentration of the composition. The greater the quantity of water added, the lower the concentration of the composition, reported in milligrams per liter (mg/l).
• an emulsifying agent such as Triton [trademark] X-100
• compositions of the present invention both the treated and untreated barley and cucumber plants were inoculated with powdery mildew fungus. This was accomplished by tapping leaves of previously infected barley and cucumber plants over the treated and untreated pots containing the barley and cucumber plants , respectively, to distribute spores of the fungus over the plants tested.
• Percent control was computed by comparing the ratings of the treated and
• each of the compounds tabulated in Table I were tested by being sprayed onto the plants as a composition, prepared in accordance with Example 5 at an emulsion composition concentration of 1,000 mg/l. Compositions of each compound were sprayed on two or three pots. A number of pots were unsprayed and thus acted as controls. That is, for each pot sprayed an unsprayed pot was utilized as a control.
• Example 6 Again, percent control was computed by comparing the treatment scores with the scores of the untreated
• compositions of the compounds of this invention prepared in accordance with Example 5.
• concentration of each composition was 1,000 mg/l.
• Sprayed and unsprayed pots of the plant were inoculated with spores of the rice blast fungus, Pyricularia oryzae. This inoculation was accomplished by preparing inoculum containing 20,000 to 30,000 spores per milliliter. The inoculum so prepared was sprayed on the plants with 1 to 2 drops of Tween [trademark] 20 surfactant (ethoxylated sorbitan monolaurate) to assure proper wetting of the inoculum onto the plant leaves.
• Tween [trademark] 20 surfactant ethoxylated sorbitan monolaurate
• the plants were incubated in a controlled environmental chamber at a humidity of 99% and a temperature of 21°C for about 24 hours to allow infection to occur.
• the plants, after 24 hours in the control chamber, were transferred to a greenhouse for six days to permit disease development to occur.
• Disease was manifested by blast lesions on the leaves.
• Disease control was calculated by either counting lesions, if infection was moderate, or evaluating by the 0 to 6 rating system defined in Example 6. The results of this test are also tabulated in Table III under the title "RCB 1000".
• Control of disease was determined by comparing treated plants with the untreated controls.
• the inoculum contained 20,000 to 30,000 spores per ml.
• the inoculum was sprayed with 1 to 2 drops of Tween [trademark] 20 surfactant (ethoxylated sorbitan monolaurate) to aid in wetting the leaves with the inoculum. All the inoculated peanut plant pots were incubated in a temperature-humidity control
• Pots were prepared such that they included 10 plants of 6 day old barley "Herta” variety. These pots were sprayed with compositions, formulated in accordance with the
• Example 5 of the compounds set forth in Table I. These pots, and a number of control pots planted with 10 "Herta" variety barley plants which were unsprayed, were inoculated with spores of the blast fungus, Pyricularia oryzae. In that Pyricularia oryzae is the same fungus utilized in Example 8, the method of inoculation was in accordance with the description given in that example.
• ALT Alternaria solani
• BOT Botrvtis ginerea
• FUS Fusarium oxysporm
• HMAY Helminthosporium maydis
• PHY Sclerotinia sclerotiorum
• SCM Sclerotium rolfsii
• CER Cercospora arachidicola
• Percent growth inhibition of each of the compounds tested was determined as a function of the difference between the radii of the treated and untreated disc for the eight fungus species. In the case of the Cercospora arachidicola (CER) fungi, scoring was done on a numerical basis as follows :

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• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Life Sciences & Earth Sciences (AREA)
• Dentistry (AREA)
• Wood Science & Technology (AREA)
• Plant Pathology (AREA)
• Health & Medical Sciences (AREA)
• Engineering & Computer Science (AREA)
• Agronomy & Crop Science (AREA)
• General Health & Medical Sciences (AREA)
• Pest Control & Pesticides (AREA)
• Zoology (AREA)
• Environmental Sciences (AREA)
• Agricultural Chemicals And Associated Chemicals (AREA)
• Plural Heterocyclic Compounds (AREA)
• Pyridine Compounds (AREA)
• Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

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• 1990
  • 1990-09-13 US US07/582,295 patent/US5061716A/en not_active Expired - Fee Related
• 1991
  • 1991-08-26 DE DE69114014T patent/DE69114014T2/de not_active Expired - Fee Related
  • 1991-08-26 CA CA002090465A patent/CA2090465A1/en not_active Abandoned
  • 1991-08-26 WO PCT/US1991/006082 patent/WO1992005155A1/en active IP Right Grant
  • 1991-08-26 ES ES91919316T patent/ES2089242T3/es not_active Expired - Lifetime
  • 1991-08-26 AT AT91919316T patent/ATE129237T1/de not_active IP Right Cessation
  • 1991-08-26 DK DK91919316.9T patent/DK0548285T3/da active
  • 1991-08-26 EP EP91919316A patent/EP0548285B1/en not_active Expired - Lifetime
  • 1991-09-04 IL IL99390A patent/IL99390A0/xx unknown
  • 1991-09-12 CN CN91108949A patent/CN1061406A/zh active Pending
  • 1991-09-12 YU YU152091A patent/YU152091A/sh unknown
  • 1991-09-12 MX MX9101066A patent/MX9101066A/es unknown
• 1996
  • 1996-01-03 GR GR960400010T patent/GR3018593T3/el unknown

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